Wang Fan-Fan, Tao Ping-Fang, Zhong Yu-Jun, Gu Yun-Qiong, Wang Cai Yi, Qin Feng
Guangxi Key Laboratory of Agricultural Resources Chemistry and Biotechnology, College of Chemistry and Food Science, Yulin Normal University, Yulin, P. R. China.
College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, People's Republic of China.
Nat Prod Res. 2024 Apr 29:1-7. doi: 10.1080/14786419.2024.2347463.
is frequently used as a traditional Chinese medicine and food supplement. Our previous study revealed that its constituent compounds were able to inhibit cancer cell proliferation. In our continuous exploration of bioactive compounds in , we isolated ten alkaloids (-), including one new natural compound (), and nine known alkaloids (), from an ethanolic extract of the whole plant. The chemical structures were elucidated based on a combination of comprehensive NMR and HRESIMS analyses. Compounds and exhibited significant antiproliferative effects against A549 cancer cell lines. We further elucidated the underlying molecular mechanisms of the antiproliferative activity of compound in A549 human lung cancer cells. Compound was found to induce cell cycle arrest in the G0/G1 phase p53 activation and CDK4/6 suppression. Compound also effectively inhibited cell migration through the modulation of the epithelial-mesenchymal transition (EMT), as indicated by the expression of biomarkers, such as N-cadherin downregulation and E-cadherin upregulation. Compound significantly suppressed the activation of the EGFR/AKT/mTOR signalling pathway in A549 cells. These results indicate that alkaloid from has potential to be a lead antiproliferative compound in cancer cells.
常被用作中药和食品补充剂。我们之前的研究表明其成分化合物能够抑制癌细胞增殖。在我们对[植物名称]中生物活性化合物的持续探索中,从全株植物的乙醇提取物中分离出了十种生物碱(-),包括一种新的天然化合物()和九种已知生物碱()。基于综合核磁共振(NMR)和高分辨电喷雾电离质谱(HRESIMS)分析相结合的方法阐明了化学结构。化合物[具体化合物编号]和[具体化合物编号]对A549癌细胞系表现出显著的抗增殖作用。我们进一步阐明了化合物[具体化合物编号]在A549人肺癌细胞中抗增殖活性的潜在分子机制。发现化合物[具体化合物编号]诱导细胞周期停滞在G0/G1期,激活p53并抑制CDK4/6。化合物[具体化合物编号]还通过调节上皮-间质转化(EMT)有效抑制细胞迁移,生物标志物的表达如N-钙黏蛋白下调和E-钙黏蛋白上调表明了这一点。化合物[具体化合物编号]显著抑制A549细胞中EGFR/AKT/mTOR信号通路的激活。这些结果表明来自[植物名称]的生物碱[具体化合物编号]有潜力成为癌细胞中一种主要的抗增殖化合物。